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1 nce of molecular motors - a process we term 'skating'.
2 the homologue in a primitive vertebrate, the skate.
3 elios, and Eos in Raja eglanteria (clearnose skate), a cartilaginous fish that is representative of a
5 e ability of the basic domain of dynactin to skate along microtubules is used by dynein to maintain l
7 rall most closely resembles mu chains of the skate and human and a new putative antigen binding molec
12 r organization in elasmobranch fish (sharks, skates, and rays) differs from that in other vertebrates
13 lved at all swimming speeds in the clearnose skate; and (iii) critical swimming protocols might misre
15 ewer recreational activities such as in-line skating, are rapidly gaining the recognition they deserv
16 fins of skates and rays, such as the little skate (Batoid, Leucoraja erinacea), show a strikingly un
19 gous sequences from tetrapods, zebrafish and skate can drive reporter gene expression in mouse limbs
20 nel and rectifying Kv channel predicted from skate (cartilaginous fish) ampullary organ electrophysio
21 long-term declines, and the largest (common skate complex) became locally extirpated (as did angelsh
22 family revealed that perch Cx35 and Cx34.7, skate Cx35, and mouse Cx36 constitute a novel gamma subg
23 critically endangered species such as common skate (Dipturus batis) and angelshark (Squatina squatina
27 OSTalpha-OSTbeta pairs from human, mouse, or skate) generated robust estrone 3-sulfate transport acti
29 protein in the KI-IOV was identified as the skate homolog of the mammalian red cell anion exchanger
31 22.5 million people participating in in-line skating in the United States in 1995, about 100,000 were
32 rentiation; it is found, in both the rat and skate, in the ventricular space that ultimately becomes
34 clasper development from pelvic fins of male skates is controlled by hormonal regulation of the Sonic
35 Further analyses showed that microtubule skating is a form of one-dimensional diffusion along the
36 s of the shark Scyliorhinus canicula and the skate Leucoraja erinacea and the absence of all HoxC gen
37 nts of the jaw, hyoid and gill arches of the skate Leucoraja erinacea derive from molecularly equival
38 expressed by electrosensory cells in little skate (Leucoraja erinacea) and functionally couple to me
39 he gills of a cartilaginous fish, the little skate (Leucoraja erinacea), are in fact endodermally der
41 DiI tracing for up to 70 days in the little skate, Leucoraja erinacea, we show that lateral line pla
45 the similarity of the cytoplasmic domains of skate opsin to those of blue-sensitive visual pigments.
50 human P2Y(2), rat P2Y(6), human P2Y(11), or skate P2Y receptors in oocytes resulted in modulation of
51 ply ancestral patterns of gene expression in skate pectoral fins, shedding light on the molecular mec
52 The 5' and 3' untranslated regions of the skate peripherin/rds (srds) cDNA were isolated by the ra
53 To determine the cellular function of the skating phenomenon, dynein and the dynactin microtubule-
55 to functionally complement the corresponding skate proteins by measuring transport of [3H]estrone 3-s
57 The tissue-specific expression patterns of skate PU.1 and Spi-C suggest that these genes share regu
58 s are highly conserved between mammalian and skate PU.1, in marked contrast to lamprey Spi, in which
59 sed a negatively buoyant fish, the clearnose skate Raja eglanteria, and took two approaches: a classi
60 heteroclitus), two elasmobranch species (the skate Raja erinacea and the dogfish Mustelus canis), and
61 ce suggests that hepatocytes from the little skate Raja erinacea express a primitive P2Y ATP receptor
62 rily primitive marine vertebrate, the little skate Raja erinacea, was screened for taurocholate trans
66 a proteins recently identified in the little skate, Raja erinacea, even though the latter exhibit onl
71 ast two of the four Ikaros family members in skate resemble the patterns observed in mammals, i.e., i
74 molecular basis of visual adaptation in the skate retina, we have cloned and analyzed the opsin cDNA
79 indicate alterations in the interactions of skate rhodopsin with other proteins in the phototransduc
81 in the posterior half of the pectoral fin of skate, shark, and zebrafish but in the anterior side of
84 on and fate-mapping approaches in the little skate to demonstrate that Shh secretion from a signallin
85 mobranch fishes, including sharks, rays, and skates, use specialized electrosensory organs called amp
86 had and whether or not they performed trick skating, was 9.5 (95 percent confidence interval, 2.6 to
87 rovided by batoid fish such as stingrays and skates, we created a biohybrid system that enables an ar
88 earned a motor skill, such as cycling or ice-skating, we can rapidly generalize to novel tasks, such
89 ically isolated external horizontal cells of skate were examined using whole-cell voltage-clamp techn
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